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Contact-independent killing mediated by a T6SS effector with intrinsic cell-entry properties

Bacterial type VI secretion systems (T6SSs) inject toxic effectors into adjacent eukaryotic and prokaryotic cells. It is generally thought that this process requires physical contact between the two cells. Here, we provide evidence of contact-independent killing by a T6SS-secreted effector. We show...

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Autores principales: Song, Li, Pan, Junfeng, Yang, Yantao, Zhang, Zhenxing, Cui, Rui, Jia, Shuangkai, Wang, Zhuo, Yang, Changxing, Xu, Lei, Dong, Tao G., Wang, Yao, Shen, Xihui
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7813860/
https://www.ncbi.nlm.nih.gov/pubmed/33462232
http://dx.doi.org/10.1038/s41467-020-20726-8
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author Song, Li
Pan, Junfeng
Yang, Yantao
Zhang, Zhenxing
Cui, Rui
Jia, Shuangkai
Wang, Zhuo
Yang, Changxing
Xu, Lei
Dong, Tao G.
Wang, Yao
Shen, Xihui
author_facet Song, Li
Pan, Junfeng
Yang, Yantao
Zhang, Zhenxing
Cui, Rui
Jia, Shuangkai
Wang, Zhuo
Yang, Changxing
Xu, Lei
Dong, Tao G.
Wang, Yao
Shen, Xihui
author_sort Song, Li
collection PubMed
description Bacterial type VI secretion systems (T6SSs) inject toxic effectors into adjacent eukaryotic and prokaryotic cells. It is generally thought that this process requires physical contact between the two cells. Here, we provide evidence of contact-independent killing by a T6SS-secreted effector. We show that the pathogen Yersinia pseudotuberculosis uses a T6SS (T6SS-3) to secrete a nuclease effector that kills other bacteria in vitro and facilitates gut colonization in mice. The effector (Tce1) is a small protein that acts as a Ca(2+)- and Mg(2+)-dependent DNase, and its toxicity is inhibited by a cognate immunity protein, Tci1. As expected, T6SS-3 mediates canonical, contact-dependent killing by directly injecting Tce1 into adjacent cells. In addition, T6SS-3 also mediates killing of neighboring cells in the absence of cell-to-cell contact, by secreting Tce1 into the extracellular milieu. Efficient contact-independent entry of Tce1 into target cells requires proteins OmpF and BtuB in the outer membrane of target cells. The discovery of a contact-independent, long-range T6SS toxin delivery provides a new perspective for understanding the physiological roles of T6SS in competition. However, the mechanisms mediating contact-independent uptake of Tce1 by target cells remain unclear.
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spelling pubmed-78138602021-01-25 Contact-independent killing mediated by a T6SS effector with intrinsic cell-entry properties Song, Li Pan, Junfeng Yang, Yantao Zhang, Zhenxing Cui, Rui Jia, Shuangkai Wang, Zhuo Yang, Changxing Xu, Lei Dong, Tao G. Wang, Yao Shen, Xihui Nat Commun Article Bacterial type VI secretion systems (T6SSs) inject toxic effectors into adjacent eukaryotic and prokaryotic cells. It is generally thought that this process requires physical contact between the two cells. Here, we provide evidence of contact-independent killing by a T6SS-secreted effector. We show that the pathogen Yersinia pseudotuberculosis uses a T6SS (T6SS-3) to secrete a nuclease effector that kills other bacteria in vitro and facilitates gut colonization in mice. The effector (Tce1) is a small protein that acts as a Ca(2+)- and Mg(2+)-dependent DNase, and its toxicity is inhibited by a cognate immunity protein, Tci1. As expected, T6SS-3 mediates canonical, contact-dependent killing by directly injecting Tce1 into adjacent cells. In addition, T6SS-3 also mediates killing of neighboring cells in the absence of cell-to-cell contact, by secreting Tce1 into the extracellular milieu. Efficient contact-independent entry of Tce1 into target cells requires proteins OmpF and BtuB in the outer membrane of target cells. The discovery of a contact-independent, long-range T6SS toxin delivery provides a new perspective for understanding the physiological roles of T6SS in competition. However, the mechanisms mediating contact-independent uptake of Tce1 by target cells remain unclear. Nature Publishing Group UK 2021-01-18 /pmc/articles/PMC7813860/ /pubmed/33462232 http://dx.doi.org/10.1038/s41467-020-20726-8 Text en © The Author(s) 2021 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Song, Li
Pan, Junfeng
Yang, Yantao
Zhang, Zhenxing
Cui, Rui
Jia, Shuangkai
Wang, Zhuo
Yang, Changxing
Xu, Lei
Dong, Tao G.
Wang, Yao
Shen, Xihui
Contact-independent killing mediated by a T6SS effector with intrinsic cell-entry properties
title Contact-independent killing mediated by a T6SS effector with intrinsic cell-entry properties
title_full Contact-independent killing mediated by a T6SS effector with intrinsic cell-entry properties
title_fullStr Contact-independent killing mediated by a T6SS effector with intrinsic cell-entry properties
title_full_unstemmed Contact-independent killing mediated by a T6SS effector with intrinsic cell-entry properties
title_short Contact-independent killing mediated by a T6SS effector with intrinsic cell-entry properties
title_sort contact-independent killing mediated by a t6ss effector with intrinsic cell-entry properties
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7813860/
https://www.ncbi.nlm.nih.gov/pubmed/33462232
http://dx.doi.org/10.1038/s41467-020-20726-8
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